APIDRA PACKAGE INSERT PDF
Apidra SoloStar Units/ml solution for injection in a pre-filled pen – Patient The Patient Information Leaflet (PIL) is the leaflet included in the pack with a. Apidra SoloStar Units/ml solution for injection in a pre-filled pen . SoloStar, the Instructions for use included in the Package leaflet must be read carefully. APIDRA [insulin glulisine injection (rDNA origin)] is a recombinant . package insert, and the pump manufacturer’s manual (see DOSAGE AND.
|Published (Last):||12 November 2015|
|PDF File Size:||5.88 Mb|
|ePub File Size:||4.46 Mb|
|Price:||Free* [*Free Regsitration Required]|
Turn the vial of insulin glulisine and syringe upside down. The American Diabetes Association ADA also states that an opened insulin vial can be kept at room temperature for approximately 1 month.
Titrate dosage according to blood glucose and A1C goals. Insulin glulisine is contraindicated for use in patients hypersensitive to the insulin or the excipients knsert the formulations.
Rotate your injection site such that each site apidga not used more than once every 1 to 2 months.
Closely monitor blood glucose in patients on concomitant insulin or insulin secretagogue therapy. Insulin glulisine is a rapid-acting insulin analog with a quicker onset and shorter duration of action compared to regular insulin.
Important information about some of the ingredients of Apidra This medicine contains less than 1 mmol 23 mg sodium per dose, i. In large doses, salicylates uncouple oxidative phosphorylation, deplete hepatic and muscle glycogen, and cause hyperglycemia and glycosuria.
Breast-feeding may decrease insulin requirements, despite the need for packagw caloric intake. Pull back the plunger of a disposable syringe to fill the syringe with an amount of air equal to your dose of NPH insulin if your dose is 30 units, pull the plunger to the 30 unit mark.
Disopyramide may enhance the hypoglycemic effects of insulin. The pen in use must not be stored in a refrigerator. In general, insulin requirements decline during the first trimester and increase during the second and third trimesters, and then decline significantly after delivery. Read apidar all of this leaflet including the Instructions for Use of Apidra SoloStar, pre-filled pen, before using this medicine because it contains important information for you.
If a patient develops hypoglycemia during treatment, adjust anti-diabetic drug regimen accordingly. Some pharmacokinetic studies have shown increased circulating levels of insulin in patients with hepatic or renal failure.
Before taking a medicine ask your doctor if it can affect your blood sugar level and what action, if any, you need to take. Twice daily insulin regimens consist of 2 subcutaneous insulin injections given per day; approximately two-thirds of the total daily insulin dose is given in the morning and one-third in the evening.
Do not throw away any medicines via wastewater or household waste. Apidra is a short-acting insulin.
Serious hypoglycaemia may cause brain damage and may be life-threatening. If you have proliferative retinopathy an eye disease related to diabetes severe hypoglycaemic attacks may cause temporary loss of vision. Moderate Coadministration of metformin with an insulin may increase the risk of hypoglycemia. Each pen contains 3 ml solution, equivalent to Units. Your insulin dose may need to be changed during pregnancy and after giving birth.
Active ingredient insulin glulisine. Take off the inner needle cap and discard it. Warning symptoms of hyperglycaemia Thirst, increased need to urinate, tiredness, dry skin, reddening of the face, loss of appetite, low blood pressure, fast heart beat and glucose and ketone bodies in urine.
Fast-Acting, Mealtime Insulin | Apidra® (insulin glulisine [rDNA origin] injection)
In addition, the use of inhaled insulin is not recommended in patients who smoke. Monitor the patient receiving glucagon for a diagnostic procedure for the desired clinical effects.
This could lead to severe hyperglycaemia very high blood sugar and ketoacidosis build-up of acid in the blood because the body is breaking down fat instead of sugar. Patients should be monitored for worsening of glycemic control if therapy with cyclosporine is initiated in patients receiving insulin.
Thirst, increased need to urinate, tiredness, dry skin, reddening of the face, loss of appetite, low blood pressure, fast heart beat and glucose and ketone bodies in urine. Always use this medicine exactly as your doctor has told you. Dosage varies depending on previous regimen, concurrent medications, lifestyle, etc.
Major Careful monitoring of blood glucose is recommended when hydroxychloroquine and antidiabetic agents, including insulins, are coadministered. In addition, angiotensin II receptor antagonists have been associated with a reduced incidence in the development of new-onset diabetes in patients with hypertension or other cardiac disease. Talk to your doctor, pharmacist or nurse before using Apidra. Monitor blood glucose for changes in glycemic control.
Apidra is an antidiabetic agent, used to reduce high blood sugar in patients with diabetes mellitus; it may be given to adults, adolescents and children, 6 years of age and older. Moderate The risk of hypoglycemia is increased when exenatide is used in combination with insulins.
Apidra SoloStar 100 Units/ml solution for injection in a pre-filled pen
The length of time an insulin can be stored while unopened is based on the expiration date. Moderate Dose reductions and increased frequency of glucose monitoring may be required when antidiabetic agents are administered with fibric acid derivatives e.
Below is a text only representation of the Patient Information Leaflet. This medicine has been prescribed for you only. Moderate Systemic bexarotene may enhance the action of insulin, resulting in hypoglycemia.
Thus, salicylates can decrease blood glucose concentrations. Make sure that the tip of the needle does not touch the NPH insulin.